Evidence map›Paper›PMID 25125687›Full record

ArticleJournal of the American Medical Informatics Association : JAMIA2015

Registration of whole immunohistochemical slide images: an efficient way to characterize biomarker colocalization.

Xavier Moles Lopez, Paul Barbot, Yves-Rémi Van Eycke, Laurine Verset, Anne-Laure Trépant, Lionel Larbanoix, Isabelle Salmon, Christine Decaestecker

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Medical Informatics Association : JAMIA, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Xavier Moles LopezLaboratories of Image, Signal Processing and Acoustics, École Polytechnique de Bruxelles, Université Libre de Bruxelles, Bruxelles, Belgium DIAPath, Center for Microscopy and Molecular Imaging (CMMI), Gosselies, Belgium.
Paul BarbotDIAPath, Center for Microscopy and Molecular Imaging (CMMI), Gosselies, Belgium.
Yves-Rémi Van EyckeDIAPath, Center for Microscopy and Molecular Imaging (CMMI), Gosselies, Belgium.
Laurine VersetDepartment of Pathology, Erasme Hospital, Bruxelles, Belgium.
Anne-Laure TrépantDepartment of Pathology, Erasme Hospital, Bruxelles, Belgium.
Lionel LarbanoixDIAPath, Center for Microscopy and Molecular Imaging (CMMI), Gosselies, Belgium.
Isabelle SalmonDIAPath, Center for Microscopy and Molecular Imaging (CMMI), Gosselies, Belgium Department of Pathology, Erasme Hospital, Bruxelles, Belgium.
Christine DecaesteckerLaboratories of Image, Signal Processing and Acoustics, École Polytechnique de Bruxelles, Université Libre de Bruxelles, Bruxelles, Belgium DIAPath, Center for Microscopy and Molecular Imaging (CMMI), Gosselies, Belgium.
VIB-UAntwerp Center for Molecular Neurology · BEErasmus Hospital · BEUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveExtracting accurate information from complex biological processes involved in diseases, such as cancers, requires the simultaneous targeting of multiple proteins and locating their respective expression in tissue samples. This information can be collected by imaging and registering adjacent sections from the same tissue sample and stained by immunohistochemistry (IHC). Registration accuracy should be on the scale of a few cells to enable protein colocalization to be assessed.

methodsWe propose a simple and efficient method based on the open-source elastix framework to register virtual slides of adjacent sections from the same tissue sample. We characterize registration accuracies for different types of tissue and IHC staining.

resultsOur results indicate that this technique is suitable for the evaluation of the colocalization of biomarkers on the scale of a few cells. We also show that using this technique in conjunction with a sequential IHC labeling and erasing technique offers improved registration accuracies. DISCUSSION: Brightfield IHC enables to address the problem of large series of tissue samples, which are usually required in clinical research. However, this approach, which is simple at the tissue processing level, requires challenging image analysis processes, such as accurate registration, to view and extract the protein colocalization information.

conclusionsThe method proposed in this work enables accurate registration (on the scale of a few cells) of virtual slides of adjacent tissue sections on which the expression of different proteins is evidenced by standard IHC. Furthermore, combining our method with a sequential labeling and erasing technique enables cell-scale colocalization.

Indexed as

Histological TechniquesImage Interpretation, Computer-AssistedImmunohistochemistryBiomarkersCellsBiomarkersBiomarkerColocalizationDigital pathologyImage registrationImmunohistochemistryWhole slide imaging

Identifiers

PMID25125687
PMCPMC4433366
OpenAlexW2166562585

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.